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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877142Generated: October 30, 2026

1,2-Dimethoxyethane → 5-(2-Fluoro-5-methoxyphenyl)-2-methylfuran-3-carbaldehyde

https://huagongshe.com/reaction/1877142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
Reactant5-Bromo-2-methylfuran-3-carbaldehydeHCID 46941673—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product5-(2-Fluoro-5-methoxyphenyl)-2-methylfuran-3-carbaldehydeHCID 8664638093.1%

Reaction Steps

A mixture of 5-bromo-2-methylfuran-3-carbaldehyde (1.3 g), 2-fluoro-5-methoxyphenylboronic acid (1.4 g), tetrakis(triphenylphosphine)palladium(0) (0.4 g), 2N aqueous sodium carbonate solution (9 mL) and 1,2-dimethoxyethane (20 mL) was stirred overnight with refluxing under an argon atmosphere. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (0% ethyl acetate/hexane to 30% ethyl acetate/hexane), and crystallized from ethyl acetate/hexane to give the title compound (1.5 g, 93%) as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-abdf8da1c86c4206bc1c870d49fcbb61
Source noteuspto-grants-2012_11